Kali Telluricosum

Product NDC
37662-3340
11-digit product format
376623340
Labeler code
37662
Product ID
37662-3340_fda9b1e2-9b93-4782-e053-6394a90ac8d3
Type
HUMAN OTC DRUG
Nonproprietary name
Kali Telluricosum
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-06-08
Substance
POTASSIUM TELLURITE
Active strength
500 [hp_C]/1
Pharmacologic classes
Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
71M41949N8POTASSIUM TELLURITE7790-58-1POTASSIUM TELLURITE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-3340-137662334001200 PELLET in 1 VIAL, GLASS (37662-3340-1) 200 pellet2023-06-08NoNoHistorical
37662-3340-237662334002500 PELLET in 1 VIAL, GLASS (37662-3340-2) 500 pellet2023-06-08NoNoHistorical
37662-3340-3376623340033000 PELLET in 1 BOTTLE, GLASS (37662-3340-3) 3000 pellet2023-06-08NoNoHistorical
37662-3340-43766233400410000 PELLET in 1 BOTTLE, GLASS (37662-3340-4) 10000 pellet2023-06-08NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Kali Telluricosum - Hahnemann Laboratories, INC.Hahnemann Laboratories, INC.2023-06-08HUMAN OTC DRUG LABEL1